Literature DB >> 1451593

Neutrophil function screening in patients with chronic granulomatous disease by a flow cytometric method.

C L Epling1, D P Stites, T M McHugh, H O Chong, L L Blackwood, D W Wara.   

Abstract

Neutrophils from patients with chronic granulomatous disease (CGD) fail to produce a significant oxidative burst following stimulation. We have evaluated the use of flow cytometry and the dye 2',7'-dichlorofluorescein diacetate (DCF) for routine screening for deficiencies of neutrophil oxidative burst. A range for DCF fluorescence for phorbol myristate acetate stimulated and non-stimulated neutrophils was established based on data from 52 healthy adults. Samples from three patients with suspected neutrophil dysfunction, three patients with X-linked CGD, and one patient with autosomal recessive (AR) CGD were evaluated with both the DCF assay and the quantitative nitroblue tetrazolium dye reduction (NBT) test. For the DCF test, the ratio of mean fluorescence intensity of stimulated to non-stimulated neutrophils was less than 5 for CGD patients and from 16 to greater than 50 for healthy individuals. With the DCF test, two populations of neutrophils could be identified in samples from four carriers of X-linked CGD, although two carriers of AR CGD had NBT and DCF results in the normal range. Our data suggest the DCF test is a sensitive and convenient method for detecting CGD.

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Year:  1992        PMID: 1451593     DOI: 10.1002/cyto.990130609

Source DB:  PubMed          Journal:  Cytometry        ISSN: 0196-4763


  9 in total

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2.  Troubleshooting the dichlorofluorescein assay to avoid artifacts in measurement of toxicant-stimulated cellular production of reactive oxidant species.

Authors:  Lauren M Tetz; Patricia W Kamau; Adrienne A Cheng; John D Meeker; Rita Loch-Caruso
Journal:  J Pharmacol Toxicol Methods       Date:  2013-02-04       Impact factor: 1.950

3.  Rapid whole-blood flow cytometry assay for diagnosis of chronic granulomatous disease.

Authors:  M R O'Gorman; V Corrochano
Journal:  Clin Diagn Lab Immunol       Date:  1995-03

4.  Chronic granulomatous disease: a review of the infectious and inflammatory complications.

Authors:  Eunkyung Song; Gayatri Bala Jaishankar; Hana Saleh; Warit Jithpratuck; Ryan Sahni; Guha Krishnaswamy
Journal:  Clin Mol Allergy       Date:  2011-05-31

5.  Chronic granulomatous disease presenting as aseptic ascites in a 2-year-old child.

Authors:  J F Moreau; John A Ozolek; P Ling Lin; Todd D Green; Elaine A Cassidy; Veena L Venkat; Andrew R Buchert
Journal:  Case Reports Immunol       Date:  2013-01-28

6.  The Mammalian circadian clock gene per2 modulates cell death in response to oxidative stress.

Authors:  Maria Chiara Magnone; Sonja Langmesser; April Candice Bezdek; Tiziano Tallone; Sandro Rusconi; Urs Albrecht
Journal:  Front Neurol       Date:  2015-01-13       Impact factor: 4.003

7.  An adult autosomal recessive chronic granulomatous disease patient with pulmonary Aspergillus terreus infection.

Authors:  Esmaeil Mortaz; Somayeh Sarhifynia; Majid Marjani; Afshin Moniri; Davood Mansouri; Payam Mehrian; Karin van Leeuwen; Dirk Roos; Johan Garssen; Ian M Adcock; Payam Tabarsi
Journal:  BMC Infect Dis       Date:  2018-11-08       Impact factor: 3.090

Review 8.  Current Flow Cytometric Assays for the Screening and Diagnosis of Primary HLH.

Authors:  Samuel Cern Cher Chiang; Jack J Bleesing; Rebecca A Marsh
Journal:  Front Immunol       Date:  2019-07-23       Impact factor: 7.561

9.  In vitro interferon γ improves the oxidative burst activity of neutrophils in patients with chronic granulomatous disease with a subtype of gp91phox deficiency.

Authors:  Serkan Filiz; Dilara F Kocacik Uygun; Sadi Köksoy; Emel Şahin; Olcay Yeğin
Journal:  Cent Eur J Immunol       Date:  2015-04-22       Impact factor: 2.085

  9 in total

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